CASE REPORT article
Front. Immunol.
Sec. Cancer Immunity and Immunotherapy
This article is part of the Research TopicEndocrine Immune-Related Toxicities during Treatment of Lung Cancer with Immune Checkpoint InhibitorsView all 3 articles
Case report: A case of diabetes mellitus and pneumonitis induced by envafolimab treatment in small cell lung cancer
Provisionally accepted- Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, China
Select one of your emails
You have multiple emails registered with Frontiers:
Notify me on publication
Please enter your email address:
If you already have an account, please login
You don't have a Frontiers account ? You can register here
In this paper, we report a case of sequential immune-related adverse events induced by envafolimab in a patient with small cell lung cancer (SCLC), including immune checkpoint inhibitor-associated diabetes mellitus (ICI-DM), diabetic ketosis (DK), and pneumonitis (CIP). A 63-year-old male with limited-stage SCLC received 4 cycles of etoposide plus carboplatin chemotherapy followed by radiotherapy, concurrent with maintenance immunotherapy using envafolimab. Eight months after initiating immunotherapy, the patient developed symptoms of dry mouth and excessive thirst. The clinical presentation was consistent with ICI-DM, though all diabetes-associated autoantibodies were negative. After achieving glycemic control with insulin, envafolimab was resumed. At 15 months, metastasis to the left submandibular region was identified and managed with localized iodine-125 seed implantation; envafolimab monotherapy was continued as maintenance treatment. Nineteen months after initiation of immunotherapy, the patient presented with chest tightness, shortness of breath, and dyspnea. Further diagnostic evaluation confirmed CIP, which improved following glucocorticoid therapy. Envafolimab was consequently suspended, and topotecan therapy was initiated for one month, but was ultimately discontinued due to financial constraints. Six months after discontinuing topotecan, the patient was readmitted due to a progressively enlarging left submandibular metastases. Laboratory findings upon admission revealed DK, which had occurred due to self-discontinuation of insulin and a switch to oral hypoglycemic agents one week ago. During hospitalization, recurrent syncope of unknown origin occurred. After clinical improvement with supportive care, anti-tumor therapy with anlotinib was initiated. Following envafolimab immunotherapy, the patient sequentially developed ICI-DM, DK and CIP. With prompt intervention, severe complications such as diabetic ketoacidosis (DKA), hyperosmolar hyperglycemic state, and respiratory failure were successfully avoided. This case underscores the importance of early recognition and management of immune-related adverse events (irAEs). The occurrence of DK after self-discontinuation of insulin highlights the necessity for long-term insulin therapy in ICI-DM. The patient remains alive with an overall survival exceeding 27 months, suggesting that ICI-DM may represent a potential prognostic biomarker for favorable outcomes in patients receiving immunotherapy.
Keywords: Diabetic ketosis, Envafolimab, immune checkpoint inhibitor-induced diabetes mellitus, immune checkpoint inhibitor-induced pneumonitis, Small Cell Lung Cancer
Received: 18 Sep 2025; Accepted: 12 Feb 2026.
Copyright: © 2026 Li, Wang, Xing, Guo and Yi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Shanyong Yi
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
